Loss of a circadian adrenal corticosterone rhythm following suprachiasmatic lesions in the rat

A retinohypothalamic projection in the rat

Moore, R. Y., & Lenn, N. J. (1972) · The Journal of Comparative Neurology · doi:10.1002/cne.901460102 · Cited by 1,263

Chronobiology

Halberg, F. E. (1969) · Annual Review of Physiology · doi:10.1146/annurev.ph.31.030169.003331 · Cited by 700

Advances in Neuroendocrinology.

Brodish, A. (1963) · JAMA · doi:10.1001/jama.1963.03710120088037 · Cited by 480

Hormone Secretion of the Anterior Pituitary Gland After Physical Interruption of All Nervous Pathways to the Hypophysiotrophic Area

Halász, B., & PUPP, L. (1965) · Endocrinology · doi:10.1210/endo-77-3-553 · Cited by 397

Visual Pathway Mediating Pineal Response to Environmental Light

Moore, R. Y., Heller, A., Wurtman, R. J., & Axelrod, J. (1967) · Science · doi:10.1126/science.155.3759.220 · Cited by 134

Central Control of the Pineal Gland: Visual Pathways

Moore, R. Y., Heller, A., Bhatnager, R. K., Wurtman, R. J., & Axelrod, J. (1968) · Archives of Neurology · doi:10.1001/archneur.1968.00470320110013 · Cited by 115

Adrenocorticotrophic Hormone Secretion in Rats after Partial or Total Deafferentation of the Medial Basal Hypothalamus

Halász, B., Slusher, M. A., & Gorski, R. A. (2008) · Neuroendocrinology · doi:10.1159/000121528 · Cited by 105

Effects of Light and Visual Stimuli on Endocrine Function

Wurtman, R. J. (1967) · Neuroendocrinology · doi:10.1016/b978-1-4832-3229-4.50009-9 · Cited by 80

Fluorimetric Analysis of Corticoids

SILBER, R. H. (1966) · Methods of biochemical analysis · doi:10.1002/9780470110324.ch3 · Cited by 60

Behavioral and neuroendocrine responses to light mediated by separate visual pathways in the rat

Chase, P. A., Seiden, L. S., & Moore, R. Y. (1969) · Physiology & Behavior · doi:10.1016/0031-9384(69)90046-8 · Cited by 18

Phenotype of Per1- and Per2- expressing neurons in the suprachiasmatic nucleus of a diurnal rodent ( Arvicanthis ansorgei ): comparison with a nocturnal species, the rat

Dardente, H., Klosen, P., Caldelas, I., Pévet, P., & Masson‐Pévet, M. (2002) · Cell and Tissue Research · doi:10.1007/s00441-002-0609-9 · Cited by 44

Chronobiology: Anatomy in time

Pauly, J. E. (1983) · American Journal of Anatomy · doi:10.1002/aja.1001680403 · Cited by 42

The Biology of the Circadian Ck1εtauMutation in Mice and Syrian Hamsters: A Tale of Two SpeciesPreprint

Loudon, A. S. I., Meng, Q., Maywood, E. S., Bechtold, D. A., Boot-Handford, R., & Hastings, M. H. (2007) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2007.72.073 · Cited by 43

The Hypothalamo–Pituitary–Liver Axis: A New Hormonal System in Control of Hepatic Steroid and Drug Metabolism

Gustafsson, J.-Α., Mode, A., Norstedt, G., Hökfelt, T. G. M., Sonnenschein, C., Eneroth, P. H. E., & Skett, P. (1980) · Biochemical Actions of Hormones · doi:10.1016/b978-0-12-452807-9.50008-5 · Cited by 42

The impact of stress and stress hormones on endogenous clocks and circadian rhythms

Ota, S. M., Kong, X., Hut, R. A., Suchecki, D., & Meerlo, P. (2021) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2021.100931 · Cited by 44

Chicken suprachiasmatic nuclei: I. Efferent and afferent connections

Cantwell, E. L., & Cassone, V. M. (2006) · The Journal of Comparative Neurology · doi:10.1002/cne.20935 · Cited by 41

Repeated psychosocial stress at night, but not day, affects the central molecular clock

Bartlang, M. S., Savelyev, S. A., Johansson, A., Reber, S. O., Helfrich‐Förster, C., & Lundkvist, G. B. S. (2014) · Chronobiology International · doi:10.3109/07420528.2014.940085 · Cited by 43

Direct effects of the light environment on daily neuroendocrine control

Paul, S., & Brown, T. M. (2019) · Journal of Endocrinology · doi:10.1530/joe-19-0302 · Cited by 42

Plasticity in the expression of the steroid receptor coactivator 1 in the Japanese quail brain: Effect of sex, testosterone, stress and time of the day

Charlier, T. D., Ball, G. F., & Balthazart, J. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2006.03.002 · Cited by 41

Involvement of the suprachiasmatic nucleus in body temperature modulation by food deprivation in rats

Liu, S., Chen, X.-M., Yoda, T., Nagashima, K., Fukuda, Y., & Kanosue, K. (2002) · Brain Research · doi:10.1016/s0006-8993(01)03374-1 · Cited by 41

The effects of aging on the circadian rhythm of serum cortisol in the dog

Palazzolo, D. L., & QUADRI, S. K. (1987) · Experimental Gerontology · doi:10.1016/0531-5565(87)90019-2 · Cited by 41

The Hamster Circadian Rhythm System Includes Nuclei of the Subcortical Visual Shell

Marchant, E. G., & Morin, L. P. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-23-10482.1999 · Cited by 41

Hypermetabolism of paraventricular hypothalamus in the congenitally helpless rat

Shumake, J., Edwards, E., & Gonzalez-Lima, F. (2001) · Neuroscience Letters · doi:10.1016/s0304-3940(01)02142-5 · Cited by 41

Circadian activity rhythms in the solitary Cape molerat (Georychus capensis: Bathyergidae) with some evidence of splitting

Lovegrove, B. G., & PAPENFUS, M. (1995) · Physiology & Behavior · doi:10.1016/0031-9384(95)00106-s · Cited by 41

Circadian differences in neuronal activity of the suprachiasmatic nucleus in brain slices prepared from photo-responsive and photo-non-responsive Djungarian hamsters.

Margraf, R. R., Złomańczuk, P., Liskin, L. A., & Lynch, G. (1991) · Brain Research · doi:10.1016/0006-8993(91)90883-w · Cited by 38

Effects of ovariectomy on the binding of [125I]-αbungarotoxin (2.2 and 3.3) to the suprachiasmatic nucleus of the hypothalamus: An in vivo autoradiographic analysis

Miller, M. M., Silver, J., & Billiar, R. B. (1982) · Brain Research · doi:10.1016/0006-8993(82)91261-6 · Cited by 40

Sucrose modifies c-fos mRNA expression in the brain of rats maintained on feeding schedules

Mitra, A., Lenglos, C., Martin, J., Mbende, N., Gagné, A., & Timofeeva, E. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2011.06.033 · Cited by 40

Circadian Plasticity in the Brain of Insects and Rodents

Krzeptowski, W., Hess, G., & Pyza, E. (2018) · Frontiers in Neural Circuits · doi:10.3389/fncir.2018.00032 · Cited by 42

Thyroid Cancer and Circadian Clock Disruption

Malaguarnera, R., Ledda, C., Filippello, A., Frasca, F., Francavilla, V. C., Ramaci, T., Parisi, M. C., Rapisarda, V., & Piro, S. (2020) · Cancers · doi:10.3390/cancers12113109 · Cited by 43

CNS control of the circadian adrenocortical rhythm

SZAFARCZYK, A., IXART, G., Alonso, G., Malaval, F., Nouguier-Soulé, J., & ASSENMACHER, I. (1983) · Journal of Steroid Biochemistry · doi:10.1016/0022-4731(83)90047-x · Cited by 40

Circadian rhythms of arginine vasopressin and vasoactive intestinal polypeptide do not depend on cytoarchitecture of dispersed cell culture of rat suprachiasmatic nucleus

Honma, S., Katsuno, Y., Tanahashi, Y., Abe, H., & Honma, K. (1998) · Neuroscience · doi:10.1016/s0306-4522(98)00078-5 · Cited by 40

Changes in Toxicity and Effectiveness with Timing of Drug Administration

Ohdo, S. (2003) · Drug Safety · doi:10.2165/00002018-200326140-00002 · Cited by 42

Serotonin concentration in individual hypothalamic nuclei of rats exposed to acute immobilization stress

Cˇulman, J., Kvetnˇanský, R., Torda, T., & Murgasˇ, K. (1980) · Neuroscience · doi:10.1016/0306-4522(80)90012-3 · Cited by 40

Review on age-related differences in non-visual effects of light: melatonin suppression, circadian phase shift and pupillary light reflex in children to older adults

Eto, T., & Higuchi, S. (2023) · Journal of PHYSIOLOGICAL ANTHROPOLOGY · doi:10.1186/s40101-023-00328-1 · Cited by 39

Daily glucocorticoids promote glioblastoma growth and circadian synchrony to the host

Gonzalez-Aponte, M. F., Damato, A. R., Simon, T., Aripova, N., Darby, F., Jeon, M. S., Luo, J. R., Rubin, J. B., & Herzog, E. D. (2024) · Cancer Cell · doi:10.1016/j.ccell.2024.11.012 · Cited by 45

Targeted mutation of the calbindin D28K gene disrupts circadian rhythmicity and entrainment

Kriegsfeld, L. J., Mei, D. F., Yan, L., Witkovsky, P., LeSauter, J., Hamada, T., & Silver, R. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06239.x · Cited by 39

Circadian ATP Release in Organotypic Cultures of the Rat Suprachiasmatic Nucleus Is Dependent on P2X7 and P2Y Receptors

Svobodová, I., Bhattaracharya, A., Ivetic, M., Bendová, Z., & Zemkova, H. W. (2018) · Frontiers in Pharmacology · doi:10.3389/fphar.2018.00192 · Cited by 39

Memory and the circadian system: Identifying candidate mechanisms by which local clocks in the brain may regulate synaptic plasticity

Hartsock, M. J., & Spencer, R. L. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.07.023 · Cited by 52

The steroid hormone of sunlight soltriol (vitamin D) as a seasonal regulator of biological activities and photoperiodic rhythms

Stumpf, W. E., & Privette, T. H. (1991) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/0960-0760(91)90074-f · Cited by 39

Regulation of Circadian Photic Responses by Nitric Oxide

Melo, L., Golombek, D. A., & Ralph, M. R. (1997) · Journal of Biological Rhythms · doi:10.1177/074873049701200404 · Cited by 39

Timing, Sleep, and Respiration in Health and Disease

Buchanan, G. F. (2013) · Progress in molecular biology and translational science · doi:10.1016/b978-0-12-396971-2.00008-7 · Cited by 40

The diurnal expression of genes encoding vasopressin and vasoactive intestinal peptide within the rat suprachiasmatic nucleus is influenced by circulating glucocorticoids

Larsen, P. J., Vrang, N., Møller, M., Jessop, D. S., Lightman, S. L., Chowdrey, H. S., & Mikkelsen, J. D. (1994) · Molecular Brain Research · doi:10.1016/0169-328x(94)90021-3 · Cited by 39

Multiple effects of circadian dysfunction induced by photoperiod shifts: Alterations in context memory and food metabolism in the same subjects

McDonald, R. J., Zelinski, E. L., Keeley, R. J., Sutherland, D., Fehr, L., & Hong, N. S. (2013) · Physiology & Behavior · doi:10.1016/j.physbeh.2013.04.010 · Cited by 39

Diurnal ACTH and plasma cortisol variations in healthy dogs and in those with pituitary-dependent Cushing’s syndrome before and after treatment with retinoic acid

Castillo, V. A., Blatter, M. F. C., Gómez, N. V., Sinatra, V., Gallelli, M. F., & Ghersevich, M. C. (2008) · Research in Veterinary Science · doi:10.1016/j.rvsc.2008.06.006 · Cited by 38

Forced Desynchrony Reveals Independent Contributions of Suprachiasmatic Oscillators to the Daily Plasma Corticosterone Rhythm in Male Rats

Wotus, C., Lilley, T. R., Neal, A. S., Suleiman, N. L., Schmuck, S. C., Smarr, B. L., Fischer, B. J., & de la Iglesia, H. O. (2013) · PLoS ONE · doi:10.1371/journal.pone.0068793 · Cited by 40

The Clock in the Brain: Neurons, Glia, and Networks in Daily Rhythms

Slat, E. A., Freeman, G. M., & Herzog, E. D. (2013) · Handbook of experimental pharmacology · doi:10.1007/978-3-642-25950-0_5 · Cited by 38

Effects of exercise with or without light exposure on sleep quality and hormone reponses

Lee, H., Kim, S., & Kim, D. (2014) · Physical Activity and Nutrition · doi:10.5717/jenb.2014.18.3.293 · Cited by 38

Mutual influence of sleep and circadian clocks on physiology and cognition

Heyde, I., Kiehn, J., & Oster, H. (2017) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2017.11.003 · Cited by 40

Development and Entrainment of the Fetal Clock in the Suprachiasmatic Nuclei: The Role of Glucocorticoids

Čečmanová, V., Houdek, P., Šuchmanová, K., Sládek, M., & Sumová, A. (2019) · Journal of Biological Rhythms · doi:10.1177/0748730419835360 · Cited by 35

Circadian rhythms and proteomics: It's all about posttranslational modifications!

Mauvoisin, D. (2019) · WIREs Systems Biology and Medicine · doi:10.1002/wsbm.1450 · Cited by 40

Circadian Regulation of Cochlear Sensitivity to Noise by Circulating Glucocorticoids

Cederroth, C. R., Park, J., Basinou, V., Weger, B. D., Tserga, E., Sarlus, H., Magnusson, A. K., Kadri, N., Gachon, F., & Canlon, B. (2019) · Current Biology · doi:10.1016/j.cub.2019.06.057 · Cited by 39

Circadian clock-controlled drug metabolism and transport

Zhao, M., Xing, H., Chen, M., Dong, D., & Wu, B. (2019) · Xenobiotica · doi:10.1080/00498254.2019.1672120 · Cited by 37

CIRCADIAN CLOCKS: WHAT MAKES THEM TICK?

Zordan, M. A., Costa, R., Macino, G., Fukuhara, C., & Tosini, G. (2000) · Chronobiology International · doi:10.1081/cbi-100101056 · Cited by 38

EFFECT OF AMINO ACIDS AND MONOAMINES ON THE NEURONAL ACTIVITY OF SUPRACHIASMATIC NUCLEUS IN HYPOTHALAMIC SLICE PREPARATIONS

Shibata, S., Liou, S. Y., & Ueki, S. (1983) · The Japanese Journal of Pharmacology · doi:10.1254/jjp.33.1225 · Cited by 38

Pathways in the forebrain of the rat concerned with the release of prolactin

TINDAL, J. S., & Knaggs, G. S. (1977) · Brain Research · doi:10.1016/0006-8993(77)90101-9 · Cited by 38

SEROTONIN INVOLVEMENT IN PITUITARY‐ADRENAL FUNCTION

Vernikos, J., Kellar, K. J., Kent, D., Gonzales, C., Berger, P. A., & Barchas, J. D. (1977) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1977.tb41879.x · Cited by 38

The influence of serotonergic inputs on peptide neurons in the rat suprachiasmatic nucleus: An immunocytochemical study

Kawakami, F., Okamura, H., Fukui, K., Yanaihara, C., Yanaihara, N., Nakajima, T., & Ibata, Y. (1985) · Neuroscience Letters · doi:10.1016/0304-3940(85)90476-8 · Cited by 38

Interplay of central and peripheral circadian clocks in energy metabolism regulation

Kolbe, I., Brehm, N., & Oster, H. (2018) · Journal of Neuroendocrinology · doi:10.1111/jne.12659 · Cited by 38

Circadian/multidien Molecular Oscillations and Rhythmicity of Epilepsy (MORE)

Bernard, C. (2020) · Epilepsia · doi:10.1111/epi.16716 · Cited by 37

Adiponectin regulates the circadian rhythm of glucose and lipid metabolism

Wada, T., Yamamoto, Y., Takasugi, Y., Ishii, H., Uchiyama, T., Saitoh, K., Suzuki, M., Uchiyama, M., Yoshitane, H., Fukada, Y., et al. (2022) · Journal of Endocrinology · doi:10.1530/joe-22-0006 · Cited by 38

Time to learn: The role of the molecular circadian clock in learning and memory

Smies, C. W., Bodinayake, K. K., & Kwapis, J. L. (2022) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2022.107651 · Cited by 35

Circadian oscillators in eukaryotes

Jolma, I. W., Lærum, O. D., Lillo, C., & Ruoff, P. (2010) · WIREs Systems Biology and Medicine · doi:10.1002/wsbm.81 · Cited by 37

The involvement of Cry1 and Cry2 genes in the regulation of the circadian body temperature rhythm in mice

Nagashima, K., Matsue, K., Konishi, M., Iidaka, C., Miyazaki, K., Ishida, N., & Kanosue, K. (2004) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00395.2004 · Cited by 37

Photoreceptors for Circadian Rhythms

Ninnemann, H. (1979) · Springer eBooks · doi:10.1007/978-1-4684-3551-1_4 · Cited by 37

Normal Physiology of ACTH and GH Release in the Hypothalamus and Anterior Pituitary in Man

Lim, C. T., & Khoo, B. C. E. (2014) · Cited by 36

Meta-analysis of transcriptomic datasets identifies genes enriched in the mammalian circadian pacemaker

Brown, L. A., Williams, J. A., Taylor, L., Thomson, R. J., Nolan, P. M., Foster, F., & Peirson, S. N. (2017) · Nucleic Acids Research · doi:10.1093/nar/gkx714 · Cited by 36

Newly identified sleep–wake and circadian circuits as potential therapeutic targets

Venner, A., Todd, W. D., Fraigne, J. J., Bowrey, H. E., Eban-Rothschild, A., Kaur, S., & Anaclet, C. (2019) · SLEEP · doi:10.1093/sleep/zsz023 · Cited by 38

Influence of the extracellular matrix on cell-intrinsic circadian clocks

Streuli, C. H., & Meng, Q. (2019) · Journal of Cell Science · doi:10.1242/jcs.207498 · Cited by 35

Feto-Maternal Crosstalk in the Development of the Circadian Clock System

Astiz, M., & Oster, H. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.631687 · Cited by 36

Identification of the suprachiasmatic nucleus venous portal system in the mammalian brain

Yao, Y., Taub, A., LeSauter, J., & Silver, R. (2021) · Nature Communications · doi:10.1038/s41467-021-25793-z · Cited by 37

Circadian rhythms of S-IgA and cortisol in whole saliva —Compensatory mechanism of oral immune system for nocturnal fall of saliva secretion—

Shirakawa, T., Mitome, M., & Oguchi, H. (2004) · Pediatric Dental Journal · doi:10.1016/s0917-2394(04)70017-8 · Cited by 36

Social stimuli fail to act as entraining agents of circadian rhythms in the golden hamster

Refinetti, R., Nelson, D., & Menaker, M. (1992) · Journal of Comparative Physiology A · doi:10.1007/bf00196900 · Cited by 36

Phase preference for the display of activity is associated with the phase of extra-suprachiasmatic nucleus oscillators within and between species

Ramanathan, C., Stowie, A. C., Smale, L., & Nunez, A. A. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.07.053 · Cited by 36

Anatomy of the Mammalian Circadian System

Gooley, J. J., & Saper, C. B. (2005) · Elsevier eBooks · doi:10.1016/b0-72-160797-7/50035-5 · Cited by 36

Peripheral Circadian Oscillators.

Brown, A. J., Pendergast, J. S., & Yamazaki, S. (2019) · PubMed · Cited by 39

Prokineticin 2 depolarizes paraventricular nucleus magnocellular and parvocellular neurons

Yuill, E. A., Hoyda, T. D., Ferri, C. C., Zhou, Q., & Ferguson, A. V. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.05293.x · Cited by 36

Meal patterns of rats with dorsomedial hypothalamic nuclei lesions or sham operations

Bellinger, L. L., Mendel, V. E., Bernardis, L. L., & Castonguay, T. W. (1986) · Physiology & Behavior · doi:10.1016/0031-9384(86)90356-2 · Cited by 36

Photic phase response curve in Octodon degus: assessment as a function of activity phase preference

Kas, M. J., & Edgar, D. M. (2000) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.2000.278.5.r1385 · Cited by 36

Chapter 19 Rhythms of inhibitory and excitatory output from the circadian timing system as revealed by in vivo microdialysis

Kalsbeek, A., & Buijs, R. M. (1996) · Progress in brain research · doi:10.1016/s0079-6123(08)60414-8 · Cited by 37

Functional absence of extraocular photoreception in hamster circadian rhythm entrainment

Meijer, J. H., Thio, B., Albus, H., Schaap, J., & Ruijs, A. C. J. (1999) · Brain Research · doi:10.1016/s0006-8993(99)01509-7 · Cited by 36

The photoneuroendocrine control of seasonal breeding in the ewe

Legan, S. J., & Winans, S. S. (1981) · General and Comparative Endocrinology · doi:10.1016/0016-6480(81)90072-1 · Cited by 36

Ventromedial and dorsomedial hypothalamic syndromes in the weanling rat: Is the “center” concept really outmoded?

Bernardis, L. L. (1985) · Brain Research Bulletin · doi:10.1016/0361-9230(85)90103-0 · Cited by 36

The circadian pacemaker generates similar circadian rhythms in the fractal structure of heart rate in humans and rats

Hu, K., Scheer, F. A. J. L., Buijs, R. M., & Shea, S. A. (2008) · Cardiovascular Research · doi:10.1093/cvr/cvn150 · Cited by 35

Recording and Analysis of Circadian Rhythms in Running-wheel Activity in Rodents

Verwey, M., Robinson, B., & Amir, S. (2013) · Journal of Visualized Experiments · doi:10.3791/50186 · Cited by 35

Interactions of Circadian Rhythmicity, Stress and Orexigenic Neuropeptide Systems: Implications for Food Intake Control

Błasiak, A., Gundlach, A. L., Hess, G., & Lewandowski, M. H. (2017) · Frontiers in Neuroscience · doi:10.3389/fnins.2017.00127 · Cited by 40

Setting the main circadian clock of a diurnal mammal by hypocaloric feeding

Mendoza, J., Gourmelen, S., Dumont, S., Ciocca, D., Pévet, P., & Challet, É. (2012) · The Journal of Physiology · doi:10.1113/jphysiol.2012.230300 · Cited by 35

Activation of suprachiasmatic nuclei and primary visual cortex depends upon time of day

Vimal, R. L. P., Pandey‐Vimal, M. C., Vimal, L. P., Frederick, B. B., Stopa, E. G., Renshaw, P. F., Vimal, S. P., & Harper, D. G. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06582.x · Cited by 36

Continuous melatonin administration accelerates resynchronization following phase shifts of a light-dark cycle

Hau, M. (1995) · Physiology & Behavior · doi:10.1016/0031-9384(95)00002-z · Cited by 35

Visual discrimination impairments after lesions in zona incerta or lateral terminal nucleus of accessory optic tract

Legg, C. R. (1979) · Brain Research · doi:10.1016/0006-8993(79)90464-5 · Cited by 35

Striatal dopamine metabolism correlated with frontotemporal glucose utilization in Alzheimer's disease: A double-tracer PET study

Meguro, K., Yamaguchi, S., Itoh, M., Fujiwara, T., & Yamadori, A. (1997) · Neurology · doi:10.1212/wnl.49.4.941 · Cited by 35

Neural Organization and Cellular Mechanisms of Circadian Pacemakers

Jacklet, J. W. (1984) · International review of cytology · doi:10.1016/s0074-7696(08)61305-4 · Cited by 35

Lesions Involving the Suprachiasmatic Nucleus Eliminate the Glucagon Response to Intracranial Injection of 2-Deoxy-D-Glucose

Yamamoto, H., Nagai, K., & Nakagawa, H. (1985) · Endocrinology · doi:10.1210/endo-117-2-468 · Cited by 35

CIRCADIAN TIMING BY ENDOGENOUS OSCILLATORS IN THE NERVOUS SYSTEM: TOWARD CELLULAR MECHANISMS

Jacklet, J. (1981) · Biological Bulletin · doi:10.2307/1540882 · Cited by 38

Influence of acoustic stimulation on the circadian and ultradian rhythm of premature infants

Dorn, F., Wirth, L., Gorbey, S., Wege, M., Zemlin, M., Maier, R. F., & Lemmer, B. (2014) · Chronobiology International · doi:10.3109/07420528.2014.948183 · Cited by 34

Potent synchronization of peripheral circadian clocks by glucocorticoid injections in PER2::LUC-Clock/Clockmice

Kamagata, M., Ikeda, Y., Sasaki, H., Hattori, Y., Yasuda, S., Iwami, S., Tsubosaka, M., Ishikawa, R., Todoh, A., Tamura, K., et al. (2017) · Chronobiology International · doi:10.1080/07420528.2017.1338716 · Cited by 34

Proteomics and circadian rhythms: It's all about signaling!

Mauvoisin, D., Dayon, L., Gachon, F., & Kussmann, M. (2014) · PROTEOMICS · doi:10.1002/pmic.201400187 · Cited by 35

Time-of-day influences on respiratory sequelae following maximal electroshock-induced seizures in mice

Purnell, B. S., Hajek, M. A., & Buchanan, G. F. (2017) · Journal of Neurophysiology · doi:10.1152/jn.00039.2017 · Cited by 34

The pupillary light reflex distinguishes between circadian and non-circadian delayed sleep phase disorder (DSPD) phenotypes in young adults

McGlashan, E. M., Burns, A. C., Murray, J. M., Sletten, T. L., Magee, M., Rajaratnam, S. M. W., & Cain, S. W. (2018) · PLoS ONE · doi:10.1371/journal.pone.0204621 · Cited by 33

Increased Cerebrospinal Fluid Amyloid-β During Sleep Deprivation in Healthy Middle-Aged Adults Is Not Due to Stress or Circadian Disruption

Blattner, M. S., Panigrahi, S. K., Toedebusch, C. D., Hicks, T. J., McLeland, J., Banks, I. R., Schaibley, C., Ovod, V., Mawuenyega, K. G., Bateman, R. J., et al. (2020) · Journal of Alzheimer s Disease · doi:10.3233/jad-191122 · Cited by 34

Programmed ageing: decline of stem cell renewal, immunosenescence, and Alzheimer's disease

Lathe, R., & Clair, D. S. (2023) · Biological reviews/Biological reviews of the Cambridge Philosophical Society · doi:10.1111/brv.12959 · Cited by 37

Circadian Misalignment and Sleep Disruption in Shift Work: Implications for Fatigue and Risk of Weight Gain and Obesity

Markwald, R. R., & Wright, K. P. (2012) · Springer eBooks · doi:10.1007/978-1-4614-3492-4_8 · Cited by 33

Circadian rhythm sleep disorders

Reid, K. J., Chang, A., & Zee, P. C. (2004) · Medical Clinics of North America · doi:10.1016/j.mcna.2004.01.010 · Cited by 36

Biological spacetime and the temporal integration of functional modules: A case study of dento–gnathic developmental timing

Boughner, J. C., & Hallgrímsson, B. (2007) · Developmental Dynamics · doi:10.1002/dvdy.21383 · Cited by 37

The Downs and Ups of Mechanistic Research: Circadian Rhythm Research as an Exemplar

Bechtel, W. (2010) · Erkenntnis · doi:10.1007/s10670-010-9234-2 · Cited by 34

Novel sources of descending input to the spinal cord of the hatchling chick

Gross, G. H., & Oppenheim, R. W. (1985) · The Journal of Comparative Neurology · doi:10.1002/cne.902320203 · Cited by 34

Elevated arylalkylamine-N-acetyltransferase (AA-NAT) gene expression in medial habenular and suprachiasmatic nuclei of hibernating ground squirrels

Yu, E. Z., Hallenbeck, J. M., Cai, D., & McCarron, R. M. (2002) · Molecular Brain Research · doi:10.1016/s0169-328x(02)00138-9 · Cited by 36

The Suprachiasmatic Nucleus

Pickard, G. E., & Sollars, P. J. (2008) · Elsevier eBooks · doi:10.1016/b978-012370880-9.00283-8 · Cited by 34

Increased neuropeptide Y concentrations in the lateral hypothalamic area of the rat after the onset of darkness: Possible relevance to the circadian periodicity of feeding behavior

McKibbin, P. E., Rogers, P., & Williams, G. H. (1991) · Life Sciences · doi:10.1016/0024-3205(91)90608-e · Cited by 34

Calbindin and Fos within the suprachiasmatic nucleus and the adjacent hypothalamus of Arvicanthis niloticus and Rattus norvegicus

Mahoney, M. M., Nunez, A. A., & Smale, L. (2000) · Neuroscience · doi:10.1016/s0306-4522(00)00212-8 · Cited by 34

Plasma hormone levels in growth-retarded rats with dorsomedial hypothalamic lesions

Bellinger, L. L., Bernardis, L. L., McCusker, R. H., & Campion, D. R. (1985) · Physiology & Behavior · doi:10.1016/0031-9384(85)90378-6 · Cited by 33

Reanalysis of primate brain circadian transcriptomics reveals connectivity-related oscillations

Lee, J., Chen, S., Monfared, R. V., Derdeyn, P., Leong, K., Chang, T. Y., Beier, K. T., Baldi, P., & Alachkar, A. (2023) · iScience · doi:10.1016/j.isci.2023.107810 · Cited by 8

Large‐scale analysis reveals spatiotemporal circadian patterns of cilia transcriptomes in the primate brain

Baldi, P., Alhassen, W., Chen, S., Nguyen, H. N., Khoudari, M., & Alachkar, A. (2021) · Journal of Neuroscience Research · doi:10.1002/jnr.24919 · Cited by 12

Identification of putative rat ribonuclease III by differential display: a novel rat mRNA expressed in a circadian manner in the rat suprachiasmatic nucleus

Bhogal, R. K., Mitchell, A., & Coen, C. W. (2004) · Molecular Brain Research · doi:10.1016/j.molbrainres.2004.07.023

Circadian rhythms and different photoresponses of Clock gene transcription in the rat suprachiasmatic nucleus and pineal gland.

Wang, G., Chun-ling, F., Li, J., Du, Y., & Tong, J. (2006) · PubMed · Cited by 2

Diurnal Patterns of Gene Expression in the Dorsal Vagal Complex and the Central Nucleus of the Amygdala – Non-rhythm-generating Brain Regions

Staehle, M. M., O’Sullivan, S. J., Vadigepalli, R., Kernan, K. F., Gonye, G. E., Ogunnaike, B. A., & Schwaber, J. S. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.00375 · Cited by 7